論文 - 土岐 力
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Clinical, cytogenetic, and molecular analyses of 17 neonates with transient abnormal myelopoiesis and nonconstitutional trisomy 21
Kentaro Yuzawa, Kiminori Terui, Tsutomu Toki, Rika Kanezaki, Akie Kobayashi, Tomohiko Sato, Takuya Kamio, Ko Kudo, Shinya Sasaki, Mikiya Endo, Shuichi Ozono, Keiko Nomura, Etsuro Ito
Pediatric Blood & Cancer 67 ( 4 ) e28188 2020年02月
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Highly sensitive detection of GATA1 mutations in patients with myeloid leukemia associated with Down syndrome by combining Sanger and targeted next generation sequencing
Kiminori Terui, Tsutomu Toki, Takashi Taga, Shotaro Iwamoto, Takako Miyamura, Daisuke Hasegawa, Hiroshi Moritake, Asahito Hama, Kentaro Nakashima, Rika Kanezaki, Ko Kudo, Akiko M. Saito, Keizo Horibe, Souichi Adachi, Daisuke Tomizawa, Etsuro Ito
Genes, Chromosomes and Cancer 59 ( 3 ) 160 - 167 2019年10月
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Integrated genetic and epigenetic analysis revealed heterogeneity of acute lymphoblastic leukemia in Down syndrome
Yasuo Kubota, Kumiko Uryu, Tatsuya Ito, Masafumi Seki, Tomoko Kawai, Tomoya Isobe, Tadayuki Kumagai, Tsutomu Toki, Kenichi Yoshida, Hiromichi Suzuki, Keisuke Kataoka, Yuichi Shiraishi, Kenichi Chiba, Hiroko Tanaka, Kentaro Ohki, Nobutaka Kiyokawa, Jiro Kagawa, Satoru Miyano, Akira Oka, Yasuhide Hayashi, Seishi Ogawa, Kiminori Terui, Atsushi Sato, Kenichiro Hata, Etsuro Ito, Junko Takita
Cancer Science 110 ( 10 ) 3358 - 3367 2019年09月
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Resistance of t(17;19)‐acute lymphoblastic leukemia cell lines to multiagents in induction therapy
Atsushi Watanabe, Takeshi Inukai, Keiko Kagami, Masako Abe, Masatoshi Takagi, Takashi Fukushima, Hiroko Fukushima, Toru Nanmoku, Kiminori Terui, Tatsuya Ito, Tsutomu Toki, Etsuro Ito, Junya Fujimura, Hiroaki Goto, Mikiya Endo, Thomas Look, Mark Kamps, Masayoshi Minegishi, Junko Takita, Toshiya Inaba, Hiroyuki Takahashi, Akira Ohara, Daisuke Harama, Tamao Shinohara, Shinpei Somazu, Hiroko Oshiro, Koshi Akahane, Kumiko Goi, Kanji Sugita
Cancer Medicine 8 ( 11 ) 5274 - 5288 2019年07月
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MYH7 mutation identified by next-generation sequencing in three infant siblings with bi-ventricular noncompaction presenting with restrictive hemodynamics: A report of three siblings with a severe phenotype and poor prognosis.
Miura F, Shimada J, Kitagawa Y, Otani K, Sato T, Toki T, Takahashi T, Yonesaka S, Mizukami H, Ito E
Journal of cardiology cases 19 ( 4 ) 140 - 143 2019年04月
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Comprehensive genetic analyses of relapsed B-cell precursor acute lymphoblastic leukemia in children
Kubo Kaori, Kudo Ko, Toki Tsutomu, Ito Etsuro, Ikeda Fumika, Ito Tatsuya, Kobayashi Akie, Sato Tomohiko, Kamio Takuya, Sasaki Shinya
Hirosaki Medical Journal 70 ( 1 ) 13 - 23 2019年
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Effective response to azacitidine in a child with a second relapse of myeloid leukemia associated with Down syndrome after bone marrow transplantation.
S. Uemura, T. Mori, C. Nagano, S. Takafuji, N. Nishimura, T. Toki, K. Terui, E. Ito, K. Iijima
Pediatric blood & cancer 65 ( 12 ) e27414 - e27414 2018年12月
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Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutation
Ko Kudo, Hiroo Ueno, Tomohiko Sato, Kaori Kubo, Rika Kanezaki, Akie Kobayashi, Takuya Kamio, Shinya Sasaki, Kiminori Terui, Akira Kurose, Kenichi Yoshida, Yusuke Shiozawa, Tsutomu Toki, Seishi Ogawa, Etsuro Ito
Genes, Chromosomes and Cancer 57 ( 12 ) 665 - 669 2018年10月
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Effective response to azacitidine in a child with a second relapse of myeloid leukemia associated with Down syndrome after bone marrow transplantation
Suguru Uemura, Takeshi Mori, China Nagano, Satoru Takafuji, Noriyuki Nishimura, Tsutomu Toki, Kiminori Terui, Etsuro Ito, Kazumoto Iijima
Pediatric Blood & Cancer 65 ( 12 ) e27414 2018年09月
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De Novo Mutations Activating Germline TP53 in an Inherited Bone-Marrow-Failure Syndrome.
Toki T, Yoshida K, Wang R, Nakamura S, Maekawa T, Goi K, Katoh MC, Mizuno S, Sugiyama F, Kanezaki R, Uechi T, Nakajima Y, Sato Y, Okuno Y, Sato-Otsubo A, Shiozawa Y, Kataoka K, Shiraishi Y, Sanada M, Chiba K, Tanaka H, Terui K, Sato T, Kamio T, Sakaguchi H, Ohga S, Kuramitsu M, Hamaguchi I, Ohara A, Kanno H, Miyano S, Kojima S, Ishiguro A, Sugita K, Kenmochi N, Takahashi S, Eto K, Ogawa S, Ito E
American journal of human genetics 103 ( 3 ) 440 - 447 2018年09月
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Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia.
Sonoda M, Ishimura M, Ichimiya Y, Terashi E, Eguchi K, Sakai Y, Takada H, Hama A, Kanno H, Toki T, Ito E, Ohga S
International journal of hematology 108 ( 2 ) 228 - 231 2018年08月
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Correction to: Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia.
Sonoda M, Ishimura M, Ichimiya Y, Terashi E, Eguchi K, Sakai Y, Takada H, Hama A, Kanno H, Toki T, Ito E, Ohga S
International journal of hematology 108 ( 2 ) 236 - 236 2018年08月
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綜説 Diamond-Blackfan貧血の診断的ターゲットおよびエクソームシーケンス解析
土岐 力, 伊藤 悦朗
小児科 59 ( 8 ) 1203 - 1212 2018年07月
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本邦におけるDiamond-Blackfan貧血の診断的ターゲットおよびエクソームシーケンス解析
土岐 力, 伊藤 悦朗
臨床血液 59 ( 7 ) 945 - 952 2018年
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Purification of leukemic blast cells from blood smears using laser microdissection.
Matsuo H, Shiga S, Imai T, Kamikubo Y, Toki T, Terui K, Ito E, Adachi S
International journal of hematology 106 ( 1 ) 55 - 59 2017年07月
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Diagnostic challenge of Diamond-Blackfan anemia in mothers and children by whole-exome sequencing.
Takuya Ichimura, Kenichi Yoshida, Yusuke Okuno, Toshiaki Yujiri, Kozo Nagai, Masanori Nishi, Yuichi Shiraishi, Hiroo Ueno, Tsutomu Toki, Kenichi Chiba, Hiroko Tanaka, Hideki Muramatsu, Toshiro Hara, Hitoshi Kanno, Seiji Kojima, Satoru Miyano, Etsuro Ito, Seishi Ogawa, Shouichi Ohga
International journal of hematology 105 ( 4 ) 515 - 520 2017年04月
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Exome sequencing identified RPS15A as a novel causative gene for Diamond-Blackfan anemia.
Fumika Ikeda, Kenichi Yoshida, Tsutomu Toki, Tamayo Uechi, Shiori Ishida, Yukari Nakajima, Yoji Sasahara, Yusuke Okuno, Rika Kanezaki, Kiminori Terui, Takuya Kamio, Akie Kobayashi, Takashi Fujita, Aiko Sato-Otsubo, Yuichi Shiraishi, Hiroko Tanaka, Kenichi Chiba, Hideki Muramatsu, Hitoshi Kanno, Shouichi Ohga, Akira Ohara, Seiji Kojima, Naoya Kenmochi, Satoru Miyano, Seishi Ogawa, Etsuro Ito
Haematologica 102 ( 3 ) e93 - e96 2017年03月
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感染を契機に診断に至ったRPL11の遺伝子変異陽性Diamond-Blackfan anemiaの11歳男児例(原著論文/症例報告)
新居 敏, 藤野 寿典, 赤澤 嶺, 田尻 雄二朗, 高野 良彦, 土岐 力, 他
小児科臨床 69 ( 8 ) 1416 - 1420 2016年08月
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Erythrocyte glutathione is a novel biomarker of Diamond-Blackfan anemia.
Utsugisawa T, Uchiyama T, Toki T, Ogura H, Aoki T, Hamaguchi I, Ishiguro A, Ohara A, Kojima S, Ohga S, Ito E, Kanno H
Blood cells, molecules & diseases 59 31 - 36 2016年07月
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Systematic Cellular Disease Models Reveal Synergistic Interaction of Trisomy 21 and GATA1 Mutations in Hematopoietic Abnormalities.
Banno K, Omori S, Hirata K, Nawa N, Nakagawa N, Nishimura K, Ohtaka M, Nakanishi M, Sakuma T, Yamamoto T, Toki T, Ito E, Yamamoto T, Kokubu C, Takeda J, Taniguchi H, Arahori H, Wada K, Kitabatake Y, Ozono K
Cell reports 15 ( 6 ) 1228 - 1241 2016年05月